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ObvioHealth at Clinical Trials Festival Asia 2023

Attending this year’s Festival? We are! And, we’d love to chat with you about ways to help optimize your clinical trials—with best-in-class tools and processes that can generate stronger evidence to support regulatory approval.

Schedule a Demo

Meet Our Experts

Don't miss your chance to learn more about optimizing DCT study designs for APAC! Schedule a meeting with one of our experts to get the conversation started.

Neil Smith

Director of Clinical Operations, APAC

Neil has 25 years of experience in clinical research. In his previous roles at Novartis, IQVIA, PPD, and Parexel Pharmaceutical, Neil led or supported all phases of regional and global HIV, oncology, and hematology trials—from start up to close out—in both South Africa and Australia.

Taylor Major

Senior Implementation Manager

Taylor has been at the forefront of designing and implementing DCTs for ObvioHealth in APAC. In their previous roles, Taylor introduced digital innovations as a multi-site coordinator and has served as a project manager for private hospital networks and oncology clinics. Taylor is currently pursuing a doctoral degree at the University of Queensland, with a thesis focused on DCTs.

About ObvioHealth

ObvioHealth is a VRO (Virtual Research Organization) working hard to make the clinical trial process easier for patients, sites, and sponsors. With average retention and ePRO compliance rates of 88% and 92% respectively, ObvioHealth knows what it takes to keep trials on track.

  • Our outstanding team of DCT specialists leverage ObvioHealth’s flexible and highly configurable second-generation DCT platform and app (ObvioGo®) to design and run smoother trials from end to end.  
  • We offer the same services as a traditional CRO, but optimized for a decentralized environment to improve both participant compliance and data integrity.
  • We know APAC! We have been running DCTs in the region since well before COVID, working with ethics committees to build localized, multi-country virtual and hybrid clinical trials that adhere to all regulatory guidelines.  
  • Our virtual site-supporting COACH (Clinical Oversight and Coordination Hub) team works with both sites and directly with patients (protocol depending) to carefully track safety and compliance and engage participants every step of the way.

Schedule a Demo

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